Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Cohesion of Cortical Language Networks During Word Processing Is Predicted by a Common Polymorphism in the SETBP1 Gene. / Rakhlin, Natalia; Landi, Nicole; Lee, Maria; Magnuson, James S.; Naumova, Oxana Yu; Ovchinnikova, Irina V.; Grigorenko, Elena L.
в: New Directions for Child and Adolescent Development, Том 2020, № 169, 2020, стр. 131-155.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Cohesion of Cortical Language Networks During Word Processing Is Predicted by a Common Polymorphism in the SETBP1 Gene
AU - Rakhlin, Natalia
AU - Landi, Nicole
AU - Lee, Maria
AU - Magnuson, James S.
AU - Naumova, Oxana Yu
AU - Ovchinnikova, Irina V.
AU - Grigorenko, Elena L.
PY - 2020
Y1 - 2020
N2 - The etiological mechanisms of the genetic underpinnings of developmental language disorder (DLD) are unknown, in part due to the behavioral heterogeneity of the disorder's manifestations. In this study, we explored an association between the SETBP1 gene (18q21.1), revealed in a genome-wide association study of DLD in a geographically isolated population, and brain network-based endophenotypes of functional intracortical coherence between major language-related brain areas. We analyzed electroencephalogram (EEG) data from thirty-nine children (twenty-three with, sixteen without DLD) aged 7.17–15.83 years acquired during an auditory picture–word matching paradigm. Variation at a single nucleotide polymorphism in the intronic region of the SETBP1 gene, rs8085464, explained 19% of the variance in intracortical network cohesion (p =.00478). This suggests that the development of these brain networks might be partially associated with the variation in SETBP1.
AB - The etiological mechanisms of the genetic underpinnings of developmental language disorder (DLD) are unknown, in part due to the behavioral heterogeneity of the disorder's manifestations. In this study, we explored an association between the SETBP1 gene (18q21.1), revealed in a genome-wide association study of DLD in a geographically isolated population, and brain network-based endophenotypes of functional intracortical coherence between major language-related brain areas. We analyzed electroencephalogram (EEG) data from thirty-nine children (twenty-three with, sixteen without DLD) aged 7.17–15.83 years acquired during an auditory picture–word matching paradigm. Variation at a single nucleotide polymorphism in the intronic region of the SETBP1 gene, rs8085464, explained 19% of the variance in intracortical network cohesion (p =.00478). This suggests that the development of these brain networks might be partially associated with the variation in SETBP1.
UR - http://www.scopus.com/inward/record.url?scp=85083949092&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/21674c4b-0cd1-3fa1-af44-2b012b2c25de/
U2 - 10.1002/cad.20331
DO - 10.1002/cad.20331
M3 - Article
C2 - 32324324
AN - SCOPUS:85083949092
VL - 2020
SP - 131
EP - 155
JO - New Directions for Child and Adolescent Development
JF - New Directions for Child and Adolescent Development
SN - 1520-3247
IS - 169
ER -
ID: 62764676